Primary Site >> Stomach Cancer
Gene >> MTHFD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216605 |
| Start | 64454825:64454825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750902671 |
| CDS Mutation | c.2668G>A |
| AA Mutation | p.Asp890Asn(p.D890N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216605 |
| Start | 64427342:64427342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1133C>T |
| AA Mutation | p.Thr378Ile(p.T378I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216605 |
| Start | 64430211:64430211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1292A>G |
| AA Mutation | p.Gln431Arg(p.Q431R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216605 |
| Start | 64400831:64400831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.80T>C |
| AA Mutation | p.Leu27Ser(p.L27S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216605 |
| Start | 64424835:64424835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.759G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216605 |
| Start | 64449559:64449559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2394G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216605 |
| Start | 64442083:64442083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143959060 |
| CDS Mutation | c.1914G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |